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Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T > C
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Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to the m.14487T>C mutation in ND6
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Prospective multicenter screening of migraine criteria in Belgian patients with epilepsy
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Prospective screening of migraine criteria in Belgian patients with epilepsy
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Outcome at 3 years of age in a population-based cohort of extremely preterm infants